Metolazone
- Product NDC
- 71335-2850
- 11-digit product format
- 713352850
- Labeler code
- 71335
- Product ID
- 71335-2850_2bb1c4a0-680d-475f-8948-a5ce516bbcaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076466
- Marketing category
- ANDA
- Marketing start
- 2003-12-19
- Substance
- METOLAZONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metolazone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOLAZONE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TZ7V40X7VX |
| Rxcui | 311671 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2850-1 | Metolazone | 100 in 1 BOTTLE | TABLET | 100 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2850-1 | 71335285001 | 100 TABLET in 1 BOTTLE (71335-2850-1) | 100 tablet | 2025-10-21 | No | No | Current |